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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414993Generated: October 29, 2026

Formic Acid → HCID 135995010, compound

https://huagongshe.com/reaction/414993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantImidazoleHCID 795—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 135995116HCID 135995116—
SolventDichloromethaneHCID 6344—
ProductHCID 135995010HCID 135995010—

Reaction Conditions

Temperature0 °C

Reaction Steps

11.3 mg (0.17 mmol) of imidazole are introduced together with 33.6 mg (0.33 mmol) of triethylamine and 7.64 mg (0.17 mmol) of formic acid into 5 ml of dichloromethane under an argon atmosphere and cooled to 0° C. Then a solution of 21.1 mg (0.17 mmol) of oxalyl chloride in dichloromethane is added dropwise, and the mixture is then stirred for 15 min. 50 mg (0.17 mmol) of 6-oxo-4-(piperazin-1-yl)-2-(3-thienylmethyl)-1,6-dihydropyrimidine-5-carbonitrile are added, and the mixture is stirred at RT overnight. It is then washed with 1 N potassium bisulphate solution, the dichloromethane phase is dried over sodium sulphate and concentrated, and the residue is flash-chromatographed on silica gel (mobile phase: dichloromethane/methanol 100:1, 80:1, 60:1). 16 mg (29% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088769B2
Source datasetuspto-grants-2012_01
ORD IDord-40bc2a14dad545c1856b03bd8fad5dc6
Source noteuspto-grants-2012_01